Dear Parent, You are invited to participate in a research project being conducted by the University of South Australia. possible participant in this study because [state why the subject was selected]. Add any declarations of interest of researchers, sponsors and institutions. Provide information regarding how participants withdraw and implication for them if they do so. Sub-headings have been provided. Researcher details. Participant Information Sheet, Version 5 Date: April 23rd, 2020 1 of 5 . Remember the aim of a PIS is to provide sufficient information, in an Student │ University of South Australia │ Email: chaky224@mymail.unisa.edu.au or Phone: +61 426 276 338 Participant Consent • I have read the Participant Information Sheet and the nature and purpose of the research project has been explained to me. We are currently studying how employees respond to workplace change in organis ations that have recently undergone merger or acquisition. Attached to this Participant Information Sheet is a Consent Form. Thank you. participant#please#contact#the#Executive#Officer#of#this#Committee,#Tel:#+61#8#8302#3118;#Email:# vicki.allen@unisa.edu.au'.# Participants#or#third#parties#who#wish#to#lodgeacomplaint#about#either#thestudy#or#theway#it#is# Information collected or used will be stored as [individually identifiable, re-identifiable or non-identifiable. Likewise individuals' responses will be kept confidential by the researcher and will (or participants will) not be identified in the reporting of the research. You will not benefit financially from your involvement in this research project even if, for example, knowledge acquired from your information proves to be of commercial value to [Company/University]. What does participation in this research involve? Reviewing HREC approving this research. 1. All group participants will be asked to maintain the confidentiality of group discussions and identity of participants. Psychology; Justice & Society Academic Unit. If data is being collected via Group discussions, this Example text could be included. It should be in plain English, using language appropriate to the target audience. We thank-you in advance for your interest and support. I have read the Information Sheet, and the nature and the purpose of the research project is clear to me. The data will be stored [provide details] in [format] for this period of time [define period of time]. Consent form will be signed prior to any study assessments being performed, Randomisation and/or the use of a control group. Your participation in this phase of the project involves completing an online survey seeking information about your language program and student participation in that program. In some cases it will be appropriate to have the information sheet translated into a language other than English, or to provide an interpreter. For example, you can request a copy of the information we hold about you. A statement informing participants how long all information collected as part of the study will be retained (for example, five years or seven years), and details of where the information will be stored and the form in which it will be stored. What happens to data already collected (whether it will be included or not), If identifiable or re-identifiable data, clarify the point up until which participants can elect to have their contributions withdrawn (for example within 2 weeks of the interview/focus group). benefit. The titles must be consistent throughout the documentation. Participant Information Sheet 1. You should adjust and populate the template to suit your project and intended audience. While it is sometimes possible to obtain oral consent for research (e.g. Include names of any sponsors and any financial benefits that might arise from the conduct of the research. If you would like to know more about your different rights or the way we use your personal information to ensure we follow It is being funded by [Name of funding organisation]. Unisa researchers: Use the Unisa logo. Email: helen.banwell@unisa.edu.au This project has been approved by the University of South Australia’s human Research Ethics Committee. If you choose to submit your name and contact details, the names of participants will be stored in a restricted key-card access facility in the School of Pharmacy and Medical Sciences, UniSA for five years. Its purpose is to help potential participants to decide whether they want to take part and to provide relevant details, including contact details. This Participant Information Sheet/Consent Form tells you about the research project. Participation in this research is voluntary. Details on the use of interpreters in the consent and/or data collection process, Venue details and a statement whether participants may choose the venue, How many people will be taking part in the project overall and at this site, Whether there are different groups e.g. Their identity can be masked if they request this. Whilst all care will be taken to maintain privacy and confidentiality, the researcher cannot guarantee anonymity and confidentiality for group discussions. PARTICIPANT INFORMATION SHEET – ONLINE PARTICIPANTS PROJECT TITLE: An Australian Rental Housing Conditions Data Infrastructure HUMAN RESEARCH ETHICS COMMITTEE APPROVAL NUMBER: H-2020-069 PRINCIPAL INVESTIGATOR: Professor Emma Baker Dear Participant, You are invited to participate in the research project described below. A Participant Information Sheet is standard for research undertaken at Australian Universities. This may help you decide if you want to take part in the research. This research is being sponsored by [Name of sponsor]. It should be in plain English, using language appropriate to the target audience. It explains the processes involved with taking part. If you decide to take part and later change your mind, you are free to withdraw from the project at any stage. Participant Information Sheet Version 3 1st Oct 2019 You have a number of rights under data protection law regarding your personal information. You are invited to participate in a research project titled: An Exploratory Study: Australian Occupational Therapists Experiences and Perceptions of Assistance Dogs. In addition to the usual information, participant information sheets for protocols involving drug therapy must include: In addition to the usual information, participant information sheets for protocols involving radiation must include the following statement. Note that it is provided here in a traditional text format, but another format may be better suited for your particular research. You are free to decline to complete the survey or to withdraw from the study at any point while completing the survey, without affecting your relationship with the researchers or the University of South Australia, either now or in the future. Ethics clearance reference number: Research permission reference number: ... Prof MA Antwi on 011-670-9391 or antwima@unisa.ac.za if you have any ethical concerns. If you have any ethical concerns about the project, or questions about your rights as a participant, please contact the Executive Officer of this Committee, Tel: + 61 8 8302 3118; Email: vicki.allen@unisa.edu.au. It may be suitable to adapt for use in other trials. The Participant Information Sheet is the document that is given to potential participants with written information about the study. If you have any ethical concerns about the project or questions about your rights as a participant, please contact the Executive Officer or this Committee, telephone +61 8 8302 3118; or email vicki.allen@unisa.edu.au. Author: acoo0107 Created Date: 11/06/2019 22:13:00 Title: Participant Information Sheet and Consent Form Guidance Document for an Interventional Study Last modified by: Marguerite Kolar If you decide to withdraw from the project, please notify a member of the research team before you withdraw. There will be no clear benefit to you from your participation in this research. Please advise the researcher if you have had any exposure to radiation for any reason in the last year. Example text (include the appropriate information for your research): This research project is being conducted by [Name of person]. Provide information on the possible risks with taking part in this research project and strategies the researchers will use to manage and/or minimise the risks. This template is to assist researchers in the development of a Participant Information Sheet and Consent Form. Participant Information Sheet [10/08/2020] Participant Information Sheet Title The National Languages Plan and Strategy Project Teacher Teacher Project Number 202799 Project Sponsor Department of Education, Skills & Employment Chief Investigators Mr Andrew Scrimgeour & Professor Anne-Marie Morgan Introduction to the National Languages Plan and Strategy Project, Before you decide to do so, it is important you understand why the research is being done and what it … Dear Participant My name is Barbara Lester. Use clear, simple English at all times and avoid abbreviations and acronyms. No publications or other public information … ��ࡱ� > �� Repetition of information throughout the participant information sheet is not necessary; it may be useful to cross-reference to other section(s) to avoid repetition. Reference to the potential benefit to others in the future may be appropriate, but should not be exaggerated. The language used throughout the form should be easily understandable. Page 4 of 6. Please do not hesitate to contact Susan or Christy if you need further information at susan.hill@unisa.edu.au christy.ward@unisa.edu.au or phone +61 419806402 What are the possible benefits of taking part? The participant information sheet is the document that explains the research project to potential participants and invites their participation. Potential participants need information on which to base their choice to take part in clinical research. If you don’t wish to take part, you don’t have to. You are not required to use the outline in the template, but all information is required. Where a control group or similar methodology is to be used in your research, you should include a statement that participants may be allocated to either a control or experimental group, and that they may not be told which of these groups they are in. If submitting your assignment in hard copy you should complete and attached this Assignment Cover Sheet Assignment cover page is the first page of an assignment. Templates (PI Sheet and Agreement Form) A participant must be informed about the purpose, methods and intended possible uses of the research, what their participation in research entails and what risks, if any, are involved, so that they can make an informed decision about … Implications can include. Consent to the use of your information as described. Investigation into Australian art that is conceptually linked with ecology and environmentalism Welcome to the entry portal for the survey on Australian art that relates to ecology and environmentalism and thank you for taking the time to consider participation in this research study. Health/Social Science Research -Adult providing own consent. [LJMU Participant Information Sheet NHS TEMPLATE v1 Feb [19] Version 5.0 date: 17/06/2019 Please note, LJMU has arranged Public Liability insurance to cover the legal liability of the University as Research Sponsor in the eventuality of harm to a research participant. number of schools or hospitals or countries involved, Whether the project involves researchers from a number of organisations working in collaboration, Whether this is a follow-on study/sub-study/extension study. Briefly describe the following aspects of your project in simple terms and in only a couple of sentences for each point: Include information and clear explanation of the following: Explain any other relevant information including: If you will use email or the internet to distribute questionnaires and receive responses, you should include the following statement in the information provided to participants: The researcher will take every care to remove any identifying material from the responses you provide as early as possible. Your participation is voluntary. immediately themselves from participation in the clinical trial. Participant Information Sheet. Participant Information Sheet. Knowing what is involved will help you decide if you want to take part in the research. Why? PARTICIPANT INFORMATION SHEET . The aim of Participant Information Sheet. Use a format that best meets the needs of your research participants, but the list below summarises the areas that need to be addressed to ensure participants are appropriately informed. Provide details about who is organising and funding the research. Participant Information Sheet and Consent Form Template. Provide information on how, and approximately when, participants will be provided with a summary of the results when the research project is completed. Any information obtained in connection with this research project that can identify you will remain confidential. What makes it stick? Participant information sheets are an important aspect for conducting studies within an organization or institution. Information sheets provide potential participants with the necessary details and explanations regarding the procedures of the study. Provide a description of measures which will be taken if the participant suffers adverse events as a result of participating in the research. Title Can the addition of metacognitive training (MCT) to treatment as usual improve treatment outcomes for adolescents with For more information about eligibility requirements, please visit www.sagaftraplans.org. Invitation You are being invited to take part in this research project. • Post each assignment in an individual Unisa. � � � � � ���� 8 T �. A feasibility study. PARTICIPANT INFORMATION SHEET . What will happen to information about me? INFORMATION FOR POTENTIAL PARTICIPANTS – PARENTS AND CARERS 1. An example participant information sheet for use in pragmatic trials is provided below. Introduction – What does my participation involve? � � ���� � � � � � � � � � � �������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������������� � �� 0 y7 bjbj�� = �{ �{ e/ �� �� �� � � recommendations for improvement to the south african information technology curriculum: a case study of new higher certificate graduates’ first year of employment If the latter, this should be used as the short title in the IRAS form. The following issues should be addressed where relevant. I, _____ (participant name), confirm that the person asking my consent to take part in this research has told me about the nature, procedure, potential benefits and anticipated inconvenience of participation. How to use the Participant Sheet Information (PI Sheet) Template. Information should be provided regarding the following: By signing the consent form you consent to the research team collecting and using information about/from you for the research project. Direct Benefit- when the participant is expected to receive . A member of the research team will inform you if there are any special requirements linked to withdrawing. A statement that all records containing personal information will remain confidential and no information which could lead to identification of any individual will be released, unless required by law OR if individuals will be able to be identified, a statement should be included making them aware of this. UNSW Sydney NSW 2052 Australia Telephone +61 2 93851000 Authorised by Deputy Vice-Chancellor (Research) UNSW CRICOS Provider Code: 00098G ABN: 57 195 873 179 If you agree to participate in this research study, the following will occur: [State your process step by Participation should be voluntary and free from coercion. I understand and agree to take part. If you do decide to take part, you will be given this Participant Information and a Consent Form to sign and you will be given a copy to keep. All participants should be given a copy of the participant information sheet, even if they are completing an online questionnaire. PARTICIPANT INFORMATION SHEET : The title could be the same as in the protocol or a simplified version understandable to a lay person. If … Before you decide, it is important that The person you may need to contact will depend on the nature of your query. In this project you will be exposed to radiation at a level considered safe for you as long as you have not also been exposed to radiation in other research projects or as a part of investigation (X-Rays) or treatment (Radiotherapy) in the past year. It explains the processes involved with taking part. and HREC Executive Officer details. contact Prof E. Mnkandla, at 011 670 9059 or mnkane@unisa.ac.za. TEMPLATE DOCUMENTS. The investigator will provide you with a full explanation of the study procedures and the purpose of the study. Participant Information Sheet as a participant please contact the Executive Officer of this Committee, tel: +61 8 8302 3118; email: vicki.allen@unisa.edu.au. Explain how it will be confidential and, if it is identifiable/re-identifiable, where it will be kept and who will have access to it]. If there are no foreseeable risks, the following statement should be included: It is not anticipated that there are any risks to participation in this study beyond those encountered in everyday life. Behaviour-Brain-Body (BBB) Research Centre. This is an internet-based survey. Please also insert the below text (verbatim) into this section: This is an example of an information sheet a student should produce to distribute to all potential research participants. I understand and agree to take part. About the research If the significant benefits from the research project are to accrue to members of society in the future and NOT to the individuals taking part in the research, this should be made clear. The entry to the survey can be found at the bottom of the Participant Information Sheet. You have been invited because [Explain reason for invitation]. No personal information about you or your students is collected. humanethics@unisa.edu.au. Participant Information Sheet 1; Version 2.0, 27 May 2014 6 of 6 beginning of the study so that we can provide you with puzzle books and newsletters about how the project is going. If you decide you want to take part in the research project, … It explains the tests and research involved. INFORMATION FOR POTENTIAL PARTICIPANTS – PARENTS AND CARERS 1. Researcher details. _____ Dr Matthew Leach Nature, number, timing and time commitment of procedures and activities, visits, questionnaires, interviews, focus groups, etc, Duration of participant’s involvement (including follow-up), Duration of the research project (if this is different from their involvement), The commitment required by the participant, Access to personal records that may be required. Participant Information Sheet/Consent Form 12th December 2017 version 3.0. V2: 22-9-2020. Thank you for taking time to read this information sheet and for participating in this study. See more ideas about print templates, sheet, downloadable templates. If you choose to submit your name and contact details, the names of participants will be stored in a restricted key-card access facility in the School of Pharmacy and Medical Sciences, UniSA for five years. Instructions for Creating a Participant Information Sheet/Consent Form ( This template is a guide only. Ask questions about anything that you don’t understand or want to know more about. If you have any ethical concerns about the project, or questions about your rights as a participant, please contact the Executive Officer of this Committee, Tel: + 61 8 8302 3118; Email: vicki.allen@unisa.edu.au. [Company/University] may benefit financially from this research project if, for example, the project assists [Company/University] in any commercial enterprise. Participant Information sheet template The following is a suggested template for participant information sheets. Participant Information Sheet - W&R Parents 180528 30/05/2018 1 UniSA, School of Education Positive Education in school communities on scale and over time. � Robert Hans You will be given a copy of this Participant Information Sheet to keep. Health/Social Science Research. For example, you can request a copy of the information we hold about you. Participant Information Sheet (PIS) Template This is not offered as a rigid template, but rather a flexible framework. Please read this information carefully. Participant Information Form Please update us every time you change your address, phone number and/or email. Researchers: This project is being undertaken as an Honours project in the Bachelor of Health Science Participant Information Sheet . The plain English title of the research project, How the project is intended to fill any gap in knowledge, How it may contribute to care or education or research in the future, Any relevant background including what is already known. 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